eMedicine Specialties > Gastroenterology > Esophagus

Esophageal Hematoma: Treatment & Medication

Author: Jennifer Lynn Bonheur, MD, Fellow, Department of Internal Medicine, Division of Gastroenterology, Lenox Hill Hospital
Coauthor(s): Klaus Radebold, MD, PhD, Research Associate, Department of Surgery, Yale University School of Medicine
Contributor Information and Disclosures

Updated: Jul 20, 2006

Treatment

Medical Care

For spontaneous intramural hematoma, conservative therapy leads to an excellent prognosis. Esophageal hematomas generally resolve within 2-3 weeks with no long-term sequelae.

  • Nothing by mouth (NPO) for the first several days. Oral intake should be reintroduced gradually. A soft diet may be started in a stable patient on days 4-6. Parenteral feeding is generally not required, as most patients are able to swallow within a few days.
  • Provide intravenous fluids while the patient is NPO and transfusion of blood if needed.
    • Acid suppression should also be considered to reduce the risk of esophageal ulceration.
    • Antiemetics are indicated as needed.
  • Correction of any coagulation abnormalities is indicated.
  • Occasionally, extensive esophageal hematomas have been treated by sclerosant injections.
    • Because this entity is so rare, a clear indication for this therapeutic approach has not yet been established.
    • Complications during endoscopic sclerotherapy include rupture of the intramural hematoma.

Surgical Care

  • Surgery is only indicated in patients with massive ongoing hematemesis. This occurred in 19% of patients, as reported in a literature review of 31 patients with esophageal hematoma.
  • Via a right thoracotomy, an esophagotomy may expose the bleeding tissue, which is then oversewn.

Consultations

  • Cardiologist
  • Gastroenterologist
  • Thoracic surgeon

Medication

Acid suppression by histamine 2 (H2)-receptor antagonists or proton pump inhibitors is useful to treat or prevent esophageal ulcerations.

Proton pump inhibitors

Inhibit gastric acid secretion by inhibition of the H+/K+/ATP-ase enzyme system in the gastric parietal cells. These agents are used in cases of severe esophagitis and in patients not responding to H2-antagonist therapy.


Omeprazole (Prilosec)

Decreases gastric acid secretion by inhibiting the parietal cell H+/K+ -ATP pump.

Adult

20-40 mg PO qd before breakfast

Pediatric

Not established

May decrease effects of itraconazole and ketoconazole; may increase toxicity of warfarin, digoxin, and phenytoin

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Bioavailability may increase in elderly patients


Lansoprazole (Prevacid)

Inhibits gastric acid secretion. Used for up to 4 wk to treat and relieve symptoms of active duodenal ulcers.

Adult

30 mg PO qd before breakfast

Pediatric

Not established

May decrease effects of ketoconazole and itraconazole; may increase theophylline clearance

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Consider adjusting dose in liver impairment. Prolonged treatment (typically > 3 years) may lead to vitamin B12 malabsorption


Rabeprazole (Aciphex)

Decreases gastric acid secretion by inhibiting the parietal cell H+/K+ -ATP pump.

Adult

20-mg tab PO qd

Pediatric

Not established

May decrease effects of itraconazole and ketoconazole; may increase toxicity of warfarin, digoxin, and phenytoin

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Symptomatic relief with proton pump inhibitors may mask symptoms of gastric malignancy Prolonged treatment (typically > 3 years) may lead to vitamin B12 malabsorption


Esomeprazole magnesium (Nexium)

S-isomer of omeprazole. Inhibits gastric acid secretion by inhibiting H+/K+ -ATP pump at secretory surface of gastric parietal cells.

Adult

20-40 mg PO qd
20-40 mg IV qd IV over 10-30 min or by injection over at least three min

Pediatric

Not established

Amoxicillin or clarithromycin may increase plasma levels of esomeprazole when used concurrently; may reduce absorption of dapsone; may increase levels of diazepam and GI absorption of digoxin; may decrease absorption of iron, ketoconazole, and itraconazole

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Symptomatic relief with proton pump inhibitors may mask symptoms of gastric malignancy Prolonged treatment (typically > 3 years) may lead to vitamin B12 malabsorption


Pantoprazole Sodium (Protonix)

Inhibits gastric acid secretion by inhibiting H+/K+ -ATP pump at secretory surface of gastric parietal cells.

Adult

40 mg PO /IV qd

Pediatric

Not established

May decrease effects of itraconazole and ketoconazole; may increase toxicity of warfarin, digoxin, and phenytoin

Hypersensitivity to pantoprazole, substituted benzamidazoles (ie, esomeprazole, lansoprazole, omeprazole, rabeprazole), or any component of the formulation

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Symptomatic relief with proton pump inhibitors may mask symptoms of gastric malignancy Prolonged treatment (typically > 3 years) may lead to vitamin B12 malabsorption

H2-receptor antagonists

Reversible competitive blockers of histamine at the H2 receptors, particularly those in the gastric parietal cells where they inhibit acid secretion. The H2 antagonists are highly selective, do not affect the H1 receptors, and are not anticholinergic agents.


Ranitidine (Zantac)

Inhibits histamine stimulation of the H2 receptor in gastric parietal cells, which in turn reduces gastric acid secretion, gastric volume, and hydrogen ion concentrations.

Adult

150 mg PO bid; not to exceed 600 mg/d
Alternatively, 50 mg/dose IV/IM q6-8h

Pediatric

Not established

May decrease effects of ketoconazole and itraconazole; may alter serum levels of ferrous sulfate, diazepam, nondepolarizing muscle relaxants, and oxaprozin

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Caution in renal or liver impairment; if changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment


Famotidine (Pepcid)

Competitively inhibits histamine at H2 receptor of gastric parietal cells, resulting in reduced gastric acid secretion, gastric volume, and hydrogen ion concentrations.

Adult

40 mg/d PO bid
Alternatively, 20 mg IV bid

Pediatric

Not established

May decrease effects of ketoconazole and itraconazole

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

If changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment


Nizatidine (Axid)

Competitively inhibits histamine at H2 receptor of gastric parietal cells, resulting in reduced gastric acid secretion, gastric volume, and hydrogen ion concentrations.

Adult

300 mg PO hs or 150 mg bid

Pediatric

Not established

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Caution in renal or liver impairment; if changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment


Cimetidine (Tagamet)

Competitively inhibits histamine at H2 receptor of gastric parietal cells, resulting in reduced gastric acid secretion, gastric volume, and hydrogen ion concentrations.

Adult

150 mg PO qid; not to exceed 600 mg/d
Alternatively, 50 mg/dose IV/IM q6-8h; not to exceed 400 mg/d

Pediatric

Not established

Can increase blood levels of theophylline, warfarin, tricyclic antidepressants, triamterene, phenytoin, quinidine, propranolol, metronidazole, procainamide, and lidocaine

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Elderly patients may experience confusional states; may cause impotence and gynecomastia in young males; may increase levels of many drugs; adjust dose or discontinue treatment if changes in renal function occur

More on Esophageal Hematoma

Overview: Esophageal Hematoma
Differential Diagnoses & Workup: Esophageal Hematoma
Treatment & Medication: Esophageal Hematoma
Follow-up: Esophageal Hematoma
References

References

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  3. Amott DH, Wright GM. Dissecting haematoma of the oesophagus masquerading as acute myocardial infarction. The Medical Journal of Australia. 2006;184 (4):182-183.

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Further Reading

Keywords

esophageal apoplexy, esophageal mucosal tears, Mallory-Weiss syndrome, transmural perforation, Boerhaave syndrome, intramural hematoma of the esophagus, esophageal perforation, mediastinitis, abscess formation, vomiting, dysphagia, odynophagia, hematemesis, severe acute chest pain

Contributor Information and Disclosures

Author

Jennifer Lynn Bonheur, MD, Fellow, Department of Internal Medicine, Division of Gastroenterology, Lenox Hill Hospital
Jennifer Lynn Bonheur, MD is a member of the following medical societies: American Gastroenterological Association, American Society for Gastrointestinal Endoscopy, New York Academy of Sciences, and Sigma Xi
Disclosure: Nothing to disclose.

Coauthor(s)

Klaus Radebold, MD, PhD, Research Associate, Department of Surgery, Yale University School of Medicine
Klaus Radebold, MD, PhD is a member of the following medical societies: American Gastroenterological Association and New York Academy of Sciences
Disclosure: Nothing to disclose.

Medical Editor

Maurice A Cerulli, MD, FACG, Chief, Division of Gastroenterology and Hepatology, Associate Professor of Clinical Medicine, Department of Internal Medicine, Division of Gastroenterology, New York Methodist Hospital, Cornell University
Maurice A Cerulli, MD, FACG is a member of the following medical societies: American College of Gastroenterology, American Gastroenterological Association, American Medical Association, and American Society for Gastrointestinal Endoscopy
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Simmy Bank, MD, Chair, Professor, Department of Internal Medicine, Division of Gastroenterology, Long Island Jewish Hospital, Albert Einstein College of Medicine
Disclosure: Nothing to disclose.

CME Editor

Alex J Mechaber, MD, FACP, Assistant Dean for Medical Curriculum, Associate Professor of Medicine, Division of General Internal Medicine, University of Miami Miller School of Medicine
Alex J Mechaber, MD, FACP is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians-American Society of Internal Medicine, and Society of General Internal Medicine
Disclosure: Nothing to disclose.

Chief Editor

Julian Katz, MD, Clinical Professor of Medicine, Drexel University College of Medicine; Consulting Staff, Department of Medicine, Section of Gastroenterology and Hepatology, Hospital of the Medical College of Pennsylvania
Julian Katz, MD is a member of the following medical societies: American College of Gastroenterology, American College of Physicians, American Gastroenterological Association, American Geriatrics Society, American Medical Association, American Society for Gastrointestinal Endoscopy, American Society of Law Medicine and Ethics, American Trauma Society, Association of American Medical Colleges, and Physicians for Social Responsibility
Disclosure: Nothing to disclose.

 
 
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